One of the most common birth defects in the world is hearing loss. Every 1,000 babies are born with permanent hearing loss in one or both ears. Hearing loss can have a significant impact on a baby's development.
CapitalBio created Hereditary #Deafness Gene Detection Item using semiconductor sequencing technology. It can identify #100 mutant sites on 18 deafness-related genes such as GJB2, SLA26A4, GJB3, MT-RNR1, and others. This detection is more than 99.9 percent accurate.
The Bioelectron gene sequencer 4000 platform was created in collaboration with Thermo Fisher. It can detect 384 samples at the same time.
Diagnostic Methods for Brain CancerApril 4, 2023Brain cancer is a very difficult-to-treat neurological disease, also known as a brain tumor. Many patients ask the question, can brain cancer be cured? The earlier brain cancer is treated, the better....view
Is a Microarray Platform Right for Gene Expression?November 10, 2023When it comes to gene expression analysis, microarray platforms are a popular choice for researchers around the world. But is a microarray platform right for your specific needs? In this article, we w...view
What Is The Nommal Metabolic Testing?March 11, 2024In the rapidly evolving landscape of healthcare diagnostics, metabolic testing has emerged as a cornerstone for understanding individual health profiles and tailoring interventions accordingly. Capita...view